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Kleber Yotsumoto Fertrin & Fernando Ferreira Costa. (2010) Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment. Expert Review of Hematology 3:4, pages 443-458.
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Giulia Hardouin, Elisa MagrinAlice Corsia, Marina Cavazzana, Annarita MiccioMichaela Semeraro. (2023) Sickle Cell Disease: From Genetics to Curative Approaches. Annual Review of Genomics and Human Genetics 24:1, pages 255-275.
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Christopher J. Bean, Sheree L. Boulet, Genyan Yang, Amanda B. Payne, Nafisa Ghaji, Meredith E. Pyle, W. Craig Hooper, Pallav Bhatnagar, Jeffrey Keefer, Emily A. Barron‐Casella, James F. Casella & Michael R. DeBaun. (2013) Acute chest syndrome is associated with single nucleotide polymorphism‐defined beta globin cluster haplotype in children with sickle cell anaemia. British Journal of Haematology 163:2, pages 268-276.
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Anthoula Chatzikyriakidou, Nikolaos Sofikitis, Vasiliki Kalfakakou, Konstantinos Siamopoulos & Ioannis Georgiou. (2006) Evidence for association of SLC7A9 gene haplotypes with cystinuria manifestation in SLC7A9 mutation carriers. Urological Research 34:5, pages 299-303.
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Meredith R. Golomb. (2005) Sickle Cell Trait Is a Risk Factor for Early Stroke. Archives of Neurology 62:11, pages 1778.
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Sharada A. Sarnaik. (2005) Sickle cell diseases: current therapeutic options and potential pitfalls in preventive therapy for transcranial Doppler abnormalities. Pediatric Radiology 35:3, pages 223-228.
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Cécile Ged, Hala Mégarbané, Eliane Chouery, Magalie Lalanne, André Mégarbané & Hubert de Verneuil. (2004) Congenital Erythropoietic Porphyria: Report of a Novel Mutation with Absence of Clinical Manifestations in a Homozygous Mutant Sibling. Journal of Investigative Dermatology 123:3, pages 589-591.
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